Onda Masanori, Willingham Mark, Nagata Satoshi, Bera Tapan K, Beers Richard, Ho Mitchell, Hassan Raffit, Kreitman Robert J, Pastan Ira
Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland 20892-4264, USA.
Clin Cancer Res. 2005 Aug 15;11(16):5840-6. doi: 10.1158/1078-0432.CCR-05-0578.
Mesothelin is a cell surface protein that is highly expressed in some malignant tumors, and is a promising target for immunotherapy. Recent data suggests that mesothelin is an adhesive protein and may have a role in the metastases of ovarian cancer. Although a few monoclonal antibodies (MAb) to mesothelin have been produced, they have limitations for the study of expression of native mesothelin because of their low affinity or reactivity only with denatured mesothelin protein. We have produced novel MAbs to mesothelin to help study mesothelin function and to develop improved diagnosis and immunotherapy of mesothelin-expressing tumors.
Mesothelin-deficient mice were immunized with plasmid cDNA encoding mesothelin, and boosted with a mesothelin-rabbit IgG Fc fusion protein prior to cell fusion. Hybridomas were screened by an ELISA using plates coated with mesothelin-Fc protein.
Seventeen hybridomas producing anti-mesothelin antibodies were established and shown to react with two epitopes on mesothelin. One group reacts with the same epitope as the low affinity antibody K1 that was originally used to identify mesothelin. The other is a new group that reacts with a new epitope. One antibody from each group was chosen for further study and shown to react strongly on ELISA, on immunohistochemistry, and by fluorescence-activated cell sorting on living cells.
Our two newly established MAbs, MN and MB, have different and useful properties compared with current antibodies used for the detection of mesothelin by immunohistochemistry, fluorescence-activated cell sorting, ELISA, and Western blotting.
间皮素是一种在某些恶性肿瘤中高表达的细胞表面蛋白,是免疫治疗的一个有前景的靶点。最近的数据表明间皮素是一种粘附蛋白,可能在卵巢癌转移中起作用。尽管已经制备了一些抗间皮素单克隆抗体(MAb),但由于它们亲和力低或仅与变性间皮素蛋白反应,在研究天然间皮素表达方面存在局限性。我们制备了新型抗间皮素单克隆抗体,以帮助研究间皮素功能,并开发针对表达间皮素肿瘤的改进诊断和免疫治疗方法。
用编码间皮素的质粒cDNA免疫间皮素缺陷小鼠,并在细胞融合前用间皮素-兔IgG Fc融合蛋白加强免疫。通过使用包被有间皮素-Fc蛋白的酶联免疫吸附测定(ELISA)筛选杂交瘤。
建立了17个产生抗间皮素抗体的杂交瘤,显示它们与间皮素上的两个表位反应。一组与最初用于鉴定间皮素的低亲和力抗体K1反应相同的表位。另一组是与新表位反应的新组。从每组中选择一种抗体进行进一步研究,结果显示其在ELISA、免疫组织化学以及对活细胞进行荧光激活细胞分选时均有强烈反应。
与目前用于通过免疫组织化学、荧光激活细胞分选、ELISA和蛋白质印迹法检测间皮素的抗体相比,我们新建立的两种单克隆抗体MN和MB具有不同且有用的特性。